Electromagnetic tracking system and methods of using same

ABSTRACT

An electromagnetic tracking system including a patient support element and an electromagnetic field generator. The patient support element is superposed relative to the electromagnetic field generator, and the electromagnetic field generator is selectively moveable relative to the patient support element.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent ApplicationNo. 61/485,582, which was filed on May 12, 2011, the disclosure of whichis hereby incorporated herein by reference in its entirety.

STATEMENT OF GOVERNMENT SUPPORT

This invention was made with United States government support underGrant R01-CA-127444, awarded by the National Institutes of Health. Thegovernment has certain rights in this invention.

FIELD

This invention relates to an electromagnetic (EM) tracking system and,more particularly, to an EM tracking system including a patient supportelement that is superposed relative to an EM field generator.

BACKGROUND

Minimally invasive, image-guided surgery (IGS) offers potential benefitsto surgeons and patients alike by providing improved visualization of asurgical target, critical structures surrounding the surgical target, aswell as the positioning of instruments used during the surgery, therebyleading to improved surgical accuracy, patient safety, patient recovery,and clinical outcome. Applications of IGS include a wide spectrum ofsurgical interventions, such as intracranial, head and neck,orthopaedic, spine, and thoracic surgeries. Among the systems enablingnext-generation IGS are intraoperative imaging systems, such as mobileC-arms capable of 3D imaging, and guidance systems that registerreal-time tracking with intraoperative images.

An integral part of IGS is the tracking system. Well known trackingsystems include the Polaris Spectra (Northern Digital (NDI), Waterloo,ON Canada), which is based on a stereoscopic infrared camera andretro-reflective markers attached to tracked tools, and theMicronTracker (Claron Technology Inc., Toronto, ON Canada), which isbased on a stereoscopic video camera and checkerboard markers. Suchsystems demonstrate excellent geometric accuracy (about 0.5-2 mm targetregistration error (TRE)) but suffer potential limitations associatedwith line of sight obstruction and the inability to track flexibledevices within the body. As a result, such optical trackers aretypically limited to externalized, rigid tools, such as, for example,rigid pointers and other devices having handles (and markers) thatremain outside the body.

The accuracy required in clinical procedures is strongly dependent onthe application and surgical site. For example, a previous geometricmodel has calculated the allowable translational and rotational errorsfor safe pedicle screw insertion to range from 0.0 mm/0.0° at the T5vertebra to 3.8 mm/22.7° at the L5 vertebra. The geometric accuracy oftracking systems achieved in practice is typically about 1.5 mm inassociation with external, rigid tools, such as, for example, rigidpointers or frames. Electromagnetic (EM) trackers provide increasedflexibility in tool design due to the use of a small EM sensor andfreedom from line-of-sight obstruction. While EM trackers can exhibitsomewhat reduced geometric accuracy (about 1-2 mm TRE for the Aurora EMtracking system, NDI) and susceptibility to EM field distortion in thepresence of metallic objects, they permit implementations on flexibleinternal devices (e.g., a bronchoscope) and have shown clinicallyacceptable accuracy under optimal conditions. Previous studies haveexamined the influence of specific application settings and the use ofspecific surgical tools on tracker position and orientation accuracy.

A conventional EM tracker arrangement places an electromagnetic fieldgenerator (EMFG) on a mechanical arm over an operating table. The EMFGis draped in proximity to the sterile field. This setup has also beenextended to C-arm cone-beam computed tomography (CBCT) by moving thetracker just outside the C-arm field-of-view (FOV). The EMFG typicallyincludes a mass of metallic coils that are not x-ray compatible,necessitating that it be moved during x-ray imaging or positioned out ofthe x-ray FOV such that the tracker FOV still encompasses the surgicalfield.

An exemplary setup of a conventional EMFG mounted at tableside is shownin FIG. 1. The setup is shown within the context of x-ray fluoroscopyand/or CBCT. The region of the patient including the surgical target isplaced within the FOV (“measurement volume”) of the EM tracker (and thefluoroscopy/CT system). The Aurora EMFG is shown (NDI, Waterloo ON),along with an EM tracker control unit, tracked wired tools, two powercables, and a serial communication cable to personal computer (PC).

This conventional EM tracker arrangement has many limitations. First,arranging essential components of the EM tracking system istime-consuming and makes operating rooms complicated—an EMFG, an EMtracker control unit, wired tracked tools, two power cables, and aserial communication cable to PC must be arranged in an operating siteso as to avoid other medical equipment. Second, the complicated setuplimits intraoperative use of image-guided surgical system—the cables,tripod, and/or support arm needed to hold the EMFG can be incompatiblewith X-ray fluoroscopy, computed tomography (CT), and/or CBCT when theEMFG is in place. Thus, the EMFG must generally be positioned outside ofthe X-ray field. Additionally, the conventional position of the EMFGover the table limits space and access to the patient. Further, mountingof the EMFG above the table on a support arm introduces potentialsterility challenges—the system must be bagged and protected fromnon-sterile exposure.

Accordingly, there is a need in the pertinent art for electromagnetictracking systems and methods that improve space and access to thepatient while preserving the sterility of the surgical field. There is afurther need in the pertinent art for electromagnetic tracking systemsand methods that are compatible with X-ray imaging techniques, therebypermitting intraoperative usage of such systems and methods.

SUMMARY

Described herein is an electromagnetic tracking system. In one example,the electromagnetic tracking system includes a patient support elementand an electromagnetic field generator. The patient support element hasa longitudinal axis, a transverse axis, and a patient contact surface.The transverse axis of the patient support table is substantiallyperpendicular to the longitudinal axis of the patient support element.The electromagnetic field generator is selectively moveable along atleast one of the longitudinal axis and the transverse axis of thepatient support table. The patient contact surface of the patientsupport element is superposed relative to at least a portion of theelectromagnetic field generator.

In another example, the electromagnetic tracking system includes apatient support table and an electromagnetic field generator. Thepatient support table has a longitudinal axis, a transverse axis, and apatient contact surface. The transverse axis of the patient supporttable is substantially perpendicular to the longitudinal axis of thepatient support table. The electromagnetic field generator isoperatively coupled to the patient support table and is selectivelymoveable along at least one of the longitudinal axis and the transverseaxis of the patient support table. The patient contact surface of thepatient support table is superposed relative to at least a portion ofthe electromagnetic field generator. The electromagnetic field generatorhas a lower surface and an upper surface.

Optionally, the electromagnetic field generator can define a centralopening through the lower surface and the upper surface of theelectromagnetic field generator.

Methods of using the electromagnetic tracking system are also disclosed.

BRIEF DESCRIPTION OF THE FIGURES

These and other features of the preferred embodiments of the inventionwill become more apparent in the detailed description in which referenceis made to the appended drawings wherein:

FIG. 1 displays a conventional setup for an electromagnetic trackingsystem, as used during a C-arm fluoroscopy and/or CBCT procedure.

FIG. 2A displays an exemplary patient support table having an integralelectromagnetic field generator, as described herein. FIG. 2B displays apartial cut-away view of the patient support table of FIG. 2A thatschematically depicts the tracking of a surgical tool by theelectromagnetic tracking system described herein.

FIG. 3A depicts an exemplary mobile C-arm for intraoperative CBCT thatis positioned relative to an electromagnetic field generator having acentral opening, as described herein. FIG. 3B depicts an exemplarypatient support table having a pair of spaced brackets for receiving anelectromagnetic field generator, as described herein. FIG. 3C depictsexemplary dimensions of the patient support table of FIG. 3B, with thedotted line indicating the sliding direction (units given in mm).

FIG. 4 depicts an exemplary electromagnetic tracking system having amobile C-arm and an electromagnetic field generator for CBCT, asdescribed herein. FIG. 4 also depicts (a) an exemplary electromagneticfield generator having a central opening, as described herein, ascompared to (b) a conventional electromagnetic field generator.

FIG. 5 depicts an exemplary electromagnetic tracking system having amobile C-arm and a close-up view of an electromagnetic field generatorhaving a central opening, as described herein.

FIG. 6A is a schematic diagram of the benchtop setup for measurement ofthe accuracy of the electromagnetic tracking systems, as describedherein. FIG. 6B illustrates the shape and dimensions of an exemplaryfield generator without a central opening (the Aurora FG, NDI) and anexemplary electromagnetic field generator having a central opening(units given in mm). FIG. 6C illustrates a 6 degrees-of-freedom EMsensor mounted on a target registration error (TRE) phantom using rigidposts and a “divot” hole at discrete locations along the x-axis, asdescribed herein.

FIG. 7 displays the dimensions of an exemplary electromagnetic fieldgenerator having a central opening as described herein.

FIG. 8A displays an experimental measurement of TRE across the field ofview (FOV) of an exemplary electromagnetic field generator having acentral opening as described herein. FIG. 8B displays CBCT imagesobtained without any field generator in the X-ray field (top image) andwith the exemplary electromagnetic field generator (with central openingdescribed herein) incorporated in a patient support table (bottomimage).

FIG. 9 depicts an experimental measurement of TRE across the FOV of anexemplary electromagnetic field generator at five “slice” locations inthe z-direction (away from the field generator). The color and diameterof each circle represent the magnitude of the TRE. Each plot shows theTRE in (x,y) “slices at various depths (z). FIG. 9A was taken at z=134±4mm; FIG. 9B was taken at z=235±4 mm; FIG. 9C was taken at z=335±4 mm;FIG. 9D was taken at z=436±5 mm; and FIG. 9E was taken at z=538±5 mm.FIG. 9F illustrates the experimental setup and the five “slice”locations.

FIG. 10 displays an experimental comparison of TRE along x, y, andz-axes between an electromagnetic field generator that lacks a centralopening and an exemplary electromagnetic field generator that has acentral opening as described herein.

FIG. 11 depicts the TRE for various registration and measurementscenarios for an exemplary electromagnetic tracking system, as describedherein.

FIG. 12 depicts CBCT images of a QRM Thorax acquired using anelectromagnetic field generator (a) without a central opening and (b)with a central opening, as described herein.

FIG. 13 depicts CBCT images acquired using an electromagnetic fieldgenerator (a-c) without a central opening and (d-f) with a centralopening, as described herein.

DETAILED DESCRIPTION

The present invention can be understood more readily by reference to thefollowing detailed description, examples, drawings, and claims, andtheir previous and following description. However, before the presentdevices, systems, and/or methods are disclosed and described, it is tobe understood that this invention is not limited to the specificdevices, systems, and/or methods disclosed unless otherwise specified,and, as such, can, of course, vary. It is also to be understood that theterminology used herein is for the purpose of describing particularaspects only and is not intended to be limiting.

The following description of the invention is provided as an enablingteaching of the invention in its best, currently known embodiment. Tothis end, those skilled in the relevant art will recognize andappreciate that many changes can be made to the various aspects of theinvention described herein, while still obtaining the beneficial resultsof the present invention. It will also be apparent that some of thedesired benefits of the present invention can be obtained by selectingsome of the features of the present invention without utilizing otherfeatures. Accordingly, those who work in the art will recognize thatmany modifications and adaptations to the present invention are possibleand can even be desirable in certain circumstances and are a part of thepresent invention. Thus, the following description is provided asillustrative of the principles of the present invention and not inlimitation thereof.

As used throughout, the singular forms “a,” “an” and “the” includeplural referents unless the context clearly dictates otherwise. Thus,for example, reference to “a splint” can include two or more suchsplints unless the context indicates otherwise.

Ranges can be expressed herein as from “about” one particular value,and/or to “about” another particular value. When such a range isexpressed, another aspect includes from the one particular value and/orto the other particular value. Similarly, when values are expressed asapproximations, by use of the antecedent “about,” it will be understoodthat the particular value forms another aspect. It will be furtherunderstood that the endpoints of each of the ranges are significant bothin relation to the other endpoint, and independently of the otherendpoint.

As used herein, the terms “optional” or “optionally” mean that thesubsequently described event or circumstance may or may not occur, andthat the description includes instances where said event or circumstanceoccurs and instances where it does not.

The word “or” as used herein means any one member of a particular listand also includes any combination of members of that list.

As used herein, a “subject” is an individual and includes, but is notlimited to, a mammal (e.g., a human, horse, pig, rabbit, dog, sheep,goat, non-human primate, cow, cat, guinea pig, or rodent), a fish, abird, a reptile or an amphibian. The term does not denote a particularage or sex. Thus, adult and newborn subjects, as well as fetuses,whether male or female, are intended to be included. A “patient” is asubject that is or may be afflicted with a disease or disorder. The term“patient” includes human and veterinary subjects. As used herein, theterm “subject” can be used interchangeably with the term “patient.”

Disclosed herein are electromagnetic tracking systems and methods thatemploy an electromagnetic field generator that is positioned beneath apatient, thereby providing improved proximity to a selected region ofthe patient. As compared to conventional electromagnetic tracking andimaging systems, this arrangement can provide a larger field of view(FOV) during various imaging procedures, including, for example, X-rayimaging and computed tomography (CT) imaging. Exemplary electromagnetictracking systems, as described further herein, can comprise coils thatare arranged along two sides of a rectangular window frame, providing acentral opening and substantially hollow side supports, which housesmall wires connecting the coils. These electromagnetic tracking systemsare X-ray compatible in standard fluoroscopic setups, standard computedtomography (CT), and rotational cone-beam computed tomography (CBCT)contexts. Optionally, the electromagnetic field generator can beincorporated into or attached to a surgical operating table, a CTscanner patient support, a radiation therapy patient support (“couch”),or other patient support table. In surgical contexts, these arrangementsreduce the amount of equipment that is introduced into a sterilesurgical field (above the level of the patient support table) andproviding a simpler, more streamlined table-side setup. Some exemplaryelectromagnetic tracking systems can comprise conventionalelectromagnetic field generators that are incorporated into a patientsupport table in this manner. The electromagnetic tracking systemsdescribed herein can be used in various applications, including, forexample and without limitation, image guided surgeries, radiotherapytreatments, image scanning processes, and the like. As compared toconventional electromagnetic tracking systems, the electromagnetictracking systems described herein offer a simpler setup, better patientaccess, more accurate tracking functionality, x-ray compatibility, andeasier sterilization.

In one aspect, and with reference to FIGS. 1-5, an electromagnetictracking system 10 can comprise a patient support element 12. In thisaspect, and as shown in FIG. 2A, the patient support element can have alongitudinal axis 14, a transverse axis 16, and a patient contactsurface 18. The longitudinal axis 14 of the patient support element 12can be substantially perpendicular to the transverse axis of the patientsupport element. In exemplary aspects, the patient support element 12can be a patient support table, such as, for example and withoutlimitation, a surgical operating table. However, it is contemplated thatthe patient support element 12 can be any element upon which any portionof the patient is positioned, including, for example, a radiotherapycouch, a scanner bed of an imaging system, and the like.

In another aspect, the electromagnetic tracking system 10 can comprisean electromagnetic field generator 30. In this aspect, theelectromagnetic field generator 30 can be selectively moveable along atleast one of the longitudinal axis 14 and the transverse axis 16 of thepatient support element 12. Thus, it is contemplated that theelectromagnetic field generator 30 can optionally be selectivelymoveable along the longitudinal axis 14 of the patient support element12. It is further contemplated that the electromagnetic field generator30 can optionally be selectively moveable along the transverse axis 16of the patient support element 12. It is still further contemplated thatthe electromagnetic field generator 30 can optionally be selectivelymoveable along both the longitudinal axis 14 and the transverse axis 16of the patient support element 12.

In a further aspect, as shown in FIGS. 2-5, the patient contact surface18 of the patient support element 12 can be superposed relative to atleast a portion of the electromagnetic field generator 30. Thus, in thisaspect, it is contemplated that the electromagnetic field generator 30can be positioned generally beneath the patient support element 12. Itis further contemplated that the patient support element 12 can bevertically spaced from the electromagnetic field generator 30 by aselected distance.

It is contemplated that the electromagnetic field generator 30 can beoperatively coupled to the patient support member 12. Optionally, inexemplary aspects, as shown in FIG. 2, the electromagnetic fieldgenerator 30 can optionally be integrally positioned within the patientsupport element 12. It is contemplated that the electromagnetic fieldgenerator 30 can be configured to move within the table to maintain thefield of view on the region of interest (e.g., the “sweet region” inwhich tracker accuracy is highest) through either selective, manualsliding of the electromagnetic field generator or automated sliding ofthe electromagnetic field generator through reading the position of atracked surgical tool. It is further contemplated that sliding of theelectromagnetic field generator 30, whether manual or automatic, can beaccomplished through the use of conventional motorized systems foreffecting longitudinal positioning of a component, including, forexample and without limitation, conveyor systems, pressurized valvesystems, and the like, which can optionally be operatively coupled to acontrol unit and/or computer as described herein. It is still furthercontemplated that integration of the electromagnetic field generator 30with a tracker control unit, cables, and the like within the table canprovide a simpler overall setup with improved sterility considerationsand better patient access (when compared to conventional electromagnetictracking systems).

In another aspect, and with reference to FIG. 2B, the patient supportelement 12 can have an undersurface 22 that cooperates with the patientcontact surface 18 to define a hollow compartment 24 that is configuredto receive the electromagnetic field generator 30 (such that theelectromagnetic field generator is positioned in between theundersurface and the patient contact surface). In this aspect, followingreceipt of the electromagnetic field generator 30 within the hollowcompartment 24, the hollow compartment can be configured to permitsliding movement of the electromagnetic field generator along at leastone of the longitudinal axis 14 of the patient support element 12 andthe transverse axis 14 of the patient support element 12 and,preferably, can permit sliding movement of the electromagnetic fieldgenerator along both the longitudinal axis and transverse axis of thepatient support element. It is contemplated that at least one sideportion of the patient support element 12 spanning between the patientcontact surface 18 and the undersurface 22 can be open and/or configuredto provide access to the electromagnetic field generator 30 followingpositioning of the electromagnetic field generator within the hollowcompartment 24. It is contemplated that the electromagnetic fieldgenerator 30 can comprise, or be coupled to, a plurality of wheels 26configured to permit sliding movement of the electromagnetic fieldgenerator along the respective axes of the patient support element 12.As shown in FIG. 2B, it is further contemplated that the electromagneticfield generator can be positioned on and/or secured to a mount 28positioned within the hollow compartment 24 such that movement of themount effects a corresponding movement of the electromagnetic fieldgenerator. The mount 28 can optionally be operatively coupled to theplurality of wheels 26.

In an additional aspect, and with reference to FIG. 3, the patientsupport element 12 can comprise a pair of spaced brackets 20 that areconfigured to slidingly receive the electromagnetic field generator 30.Thus, in this aspect, the electromagnetic field generator 30 can beconfigured to slide within the spaced brackets 20. Optionally, the pairof spaced brackets 20 can extend substantially parallel to thelongitudinal axis 14 of the patient support element 12. Alternatively,it is further contemplated that the pair of spaced brackets 20 canoptionally extend substantially parallel to the transverse axis 16 ofthe patient support element 12. In exemplary aspects, it is contemplatedthat the relative positions of the brackets 20, such as, for example,the space between opposed brackets, can be selectively adjusted. It isfurther contemplated that the brackets 20 can comprise non-metallicmaterials, such as, for example and without limitation, acrylic and/orplastic materials, to thereby avoid electromagnetic field distortion andprovide x-ray compatibility. For example, it is contemplated thatbrackets 20 formed of plastic materials will not absorb x-rays, therebyensuring x-ray compatibility. As used herein, the term “bracket”includes any bracket, rail, or other elongate element defining alongitudinal channel that is configured to slidingly receive anelectromagnetic field generator 30, as described herein. It iscontemplated that the electromagnetic field generator can comprise, orbe coupled to, a plurality of wheels 26 configured to permit slidingmovement of the electromagnetic field generator within the brackets 20along the respective axes of the patient support element 12. Optionally,the electromagnetic field generator 30 can be positioned on and/orsecured to a mount 28 positioned within the brackets 20 such thatmovement of the mount effects a corresponding movement of theelectromagnetic field generator. It is further contemplated that themount 28 can optionally be operatively coupled to the plurality ofwheels 26.

In one aspect, and with reference to FIG. 5, the electromagnetic fieldgenerator 30 can have a lower surface 32 and an upper surface 34. Inthis aspect, the electromagnetic field generator 30 can optionallydefine a central opening 36 through the lower surface 32 and the uppersurface 34 of the electromagnetic field generator. It should beappreciated that, unlike the conventional electromagnetic fieldgenerator depicted in FIG. 4 (b), which is not X-ray compatible due to amass of metallic materials at the center of the field generator, thecentral opening can provide X-ray compatibility for the electromagneticfield generator depicted in FIG. 5.

In an additional aspect, it is contemplated that the electromagnetictracking system 10 can further comprise a releasable locking assemblyfor securing the electromagnetic field generator 30 in a desiredlocation following selective movement of the field generator along oneor more of the axes of the patient support element 12. For example, itis contemplated that the releasable locking assembly can comprise aplurality of screws that can cooperate with the hollow compartment 24 orthe brackets 20 to securely lock the field generator 30 in the desiredlocation during an imaging procedure. However, it is contemplated thatany conventional means for securing one element in a longitudinalposition can be used to secure the electromagnetic field generator 30 inthe desired location.

In various aspects, the electromagnetic field generator 30 can comprisea plurality of coils that are spaced so as to permit transmission ofradiation through the electromagnetic field generator without contactingthe plurality of coils, thereby preserving x-ray compatibility. In oneexemplary aspect, the plurality of coils can be spaced about the centralopening 36 of the electromagnetic field generator 30. In anotherexemplary aspect, when the electromagnetic field generator 30 isintegrally positioned within the patient support element 12, it iscontemplated that the plurality of coils can be spaced about a peripheryof the patient support element.

In another aspect, the electromagnetic field generator 30 can comprise afirst coil assembly 38 and a second coil assembly 40. In this aspect,the first coil assembly 38 can be in electrical communication with thesecond coil assembly 40. In exemplary aspects, the first and second coilassemblies 38, 40 can comprise at least one coil. Optionally, in theseaspects, the at least one coil of the first and second coil assemblies38, 40 can comprise a plurality of coils. In a particular exemplaryaspect, the first and second coil assemblies 38, 40 comprise a pluralityof spaced coils. With reference to FIG. 5, it is contemplated that thefirst coil assembly 38 and the second coil assembly 40 can both comprisea plurality of coils, with the plurality of coils of the first coilassembly being spaced along an axis substantially parallel to an axisalong which the plurality of coils of the second coil assembly 40 arespaced. Optionally, the plurality of coils of the first and second coilassemblies 38, 40 can be spaced along an axis that is substantiallyparallel to the longitudinal axis 14 of the patient support element 12.Alternatively, the plurality of coils of the first and second coilassemblies 38, 40 can be spaced along an axis that is substantiallyparallel to the transverse axis 16 of the patient support element 12. Itis further contemplated that the first coil assembly 38 can be inopposed spaced relation to the second coil assembly 40 across thecentral opening 36 of the electromagnetic field generator 30.

In a further aspect, as shown in FIGS. 3 and 5, the electromagneticfield generator 30 can further comprise first and second coil housingarms 42, 44 and first and second side arms 46, 48. In this aspect, thefirst and second coil housing arms 42, 44 and the first and second sidearms 46, 48 can cooperate to define the central opening 36 of theelectromagnetic field generator 30. It is contemplated that the firstcoil assembly 38 can be positioned with the first coil housing arm 42,while the second coil assembly 40 can be positioned within the secondcoil housing arm 44. It is still further contemplated that the first andsecond side arms 46, 48 can be connected to and oriented substantiallyperpendicularly to the first and second coil housing arms 42, 44. Inexemplary aspects, the first and second side arms 46, 48 of theelectromagnetic field generator 30 can be substantially hollow. It iscontemplated that, during an imaging procedures, although the hollowside arms are visible in oblique and lateral x-ray projections, theypresent fairly low attenuation. In additional optional, exemplaryaspects, it is contemplated that the first and second side arms 46, 48can be formed to have smooth and/or rounded corners, thereby reducingartifact during imaging procedures. In an additional aspect, the firstand second side arms 46, 48 of the electromagnetic field generator 30can comprise plastic materials, thereby avoiding electromagnetic fielddistortion and providing x-ray compatibility. In exemplary aspects, theside arms 46, 48 can define respective side edges, and at least aportion of the side edges of each side arm can be rounded. In theseaspects, it is contemplated that the absence of sharp edges in theelectromagnetic field generator 30 can reduce artifact within imagesobtained using the claimed electromagnetic tracking system 10.

In further aspects, it is contemplated that the electromagnetic fieldgenerator 30 can comprise one or more radio-translucent materials. Inthis aspect, as one will appreciate, the radio-translucentcharacteristics of the electromagnetic field generator render theelectromagnetic field generator suitable for usage with X-ray devicesand other radiation sources. In one exemplary aspect, it is contemplatedthat the electromagnetic field generator 30 can comprise aradio-translucent sheet having a periphery surrounding a central region.In this aspect, it is contemplated that the plurality of coils of theelectromagnetic field generator 30 can be spaced about the centralregion within the periphery of the radio-translucent sheet. It isfurther contemplated that the spacing of the plurality of coils aboutthe central region can be configured to permit transmission of radiationthrough the central region without contacting the plurality of coils.

In various aspects, the electromagnetic tracking system 10 can furthercomprise a radiation source 50, such as, for example and withoutlimitation, an X-ray source, a CT machine, a positron emissiontomography (PET) scanner, a radiation therapy treatment system, and thelike. Thus, it is contemplated that the radiation source 50 can be animaging device and/or a therapy device. Optionally, it is contemplatedthat the radiation source 50 can be configured to selectively transmitradiation toward the patient (such as, for example, in X-ray, CT, orCBCT procedures). It is further contemplated that the radiation source50 can be selectively positioned such that radiation can be deliveredthrough the central opening 36 and/or the hollow side arms 46, 48 of anexemplary electromagnetic field generator 30, as described herein. In anexemplary aspect, as shown in FIG. 4, the radiation source 50 cancomprise a detector 52 configured to receive radiation transmittedthrough the patient and convert the received radiation into an outputimage. In this aspect, it is contemplated that the detector 52 can be aflat panel detector. However, it is contemplated that any conventionalimaging detector can be used in the described electromagnetic trackingsystem 10. In another aspect, and with reference to FIG. 4, theradiation source 50 can further comprise a C-arm, such as those usedduring conventional X-ray, CT, and/or CBCT procedures.

In an additional aspect, the electromagnetic tracking system 10 canfurther comprise a control unit 60. In this aspect, the control unit 60can be in electrical communication with one or more of: the imagingdevice; the electromagnetic field generator; a computer; a surgicaltool, and electromagnetic sensor connectors. In exemplary aspects, asshown in FIG. 2B, it is contemplated that the control unit 60 can beincorporated directly into the patient support element 12.

In an exemplary configuration, the control unit 60 can be in electricalcommunication with a computer workstation through an interface. Theelectrical communication between the control unit 60 and the computerworkstation can occur through various communication protocols,including, for example and without limitation, Ethernet, serial cableconnections, universal serial bus (USB) connections, firewireconnections, and/or Bluetooth. It is contemplated that the computer canhave a processor that is configured to transmit signals indicative ofoperation, data sampling, and other information to the control unit 60.It is further contemplated that the computer can be configured toreceive signals from the control unit 60 indicative of system operation,timing, and the state, position, and/or orientation of tracked surgicalinstruments. Optionally, it is contemplated that the control unit 60 canbe in electrical communication with the radiation source 50 for purposesof synchronizing the tracking, imaging, and/or treatment operations ofthe system 10 and/or to direct the operation of the radiation source inresponse to information received from the computer and/or other elementsof the tracking system, such as a tracked surgical instrument.

In use, the electromagnetic tracking system 10 can be used in anelectromagnetic tracking method. In one aspect, the electromagnetictracking method can comprise positioning a patient on the patientsupport element. In another aspect, the electromagnetic tracking methodcan comprise positioning the electromagnetic field generator such thatthe patient contact surface of the patient support element is superposedrelative to at least a portion of the electromagnetic field generator.In an additional aspect, the electromagnetic tracking method cancomprise positioning an imaging source at a selected orientationrelative to the electromagnetic field generator. In this aspect, whenthe electromagnetic field generator defines a central opening asdescribed herein, the step of positioning the imaging device at theselected orientation can comprise positioning the imaging device suchthat radiation is selectively transmittable through at least one of (a)the central opening of the electromagnetic field generator and (b) thefirst and second hollow side arms of the electromagnetic fieldgenerator. In a further aspect, the electromagnetic tracking method cancomprise selectively activating the imaging device. In still a furtheraspect, the electromagnetic tracking method can comprise selectivelyactivating the electromagnetic field generator.

Optionally, in an additional aspect, the electromagnetic tracking methodcan comprise selectively moving the electromagnetic field generatoralong at least one of the longitudinal axis and the transverse axis ofthe patient support element. In this aspect, it is contemplated thatsuch movement of the electromagnetic field generator can be accomplishedmanually. However, in exemplary aspects, it is contemplated thatmovement of the electromagnetic field generator can occur automaticallydepending upon the positioning of a surgical tool that is tracked by theelectromagnetic tracking system. In these aspects, it is contemplatedthat the tracked surgical tool can comprise a tool body enclosing atleast one electromagnetic sensor. It is further contemplated that thetracked surgical tool can be in electrical communication with thecontrol unit via a data cable such that signals produced by theelectromagnetic sensor(s) within the tool body are transmitted to thecontrol unit.

When the electromagnetic tracking system comprises a C-arm, theelectromagnetic tracking method can optionally comprise registering theC-arm and tracker coordinate systems (i.e., frames of references(x,y,z)_(image), relating to the radiation source (imaging system), and(x,y,z)_(tracker), relating to the tracking system). It is contemplatedthat registration of the imaging and tracking systems can permit theposition of a tracked instrument (e.g., a surgical device tracked withinor about the patient and tracked in (x,y,z)_(tracker)) to be related toa corresponding position in the image (x,y,z)_(image). Thus, it iscontemplated that a tracked instrument, such as a surgical tool, can bevisualized within the context of the image. It is further contemplatedthat registration of the tracker and image reference frames can followany of various processes common to surgical navigation. For example andwithout limitation, it is contemplated that selection of three or moregeometric points in the world (tracker) reference frame and thecorresponding points in the image reference frame can allow forcalculation of the mathematical transformation that relates the positionin one reference frame to a corresponding position in the otherreference frame. In exemplary aspects, this can be accomplished byplacing a tracked pointer at a point in the world (tracker) coordinatesystem that can be correspondingly localized in the image coordinatesystem and then repeating this three or more times to compute thetransform. Similarly, it is contemplated that a tracked tool can be usedto trace a surface in the world (tracker) coordinate system—e.g., theexternal contour of the patient—and then correlated to the correspondingsurface in the image coordinate system by a mathematical registration ofsurfaces to determine the transform.

It is contemplated that the performance of the electromagnetic trackingsystem 10 can be affected by the proximity of metallic structures, suchas, for example, large surgical instruments, a C-arm, a CT scanner, andthe like. To allow more accurate tracker-to-image registration in thepresence of such systems about the electromagnetic field generator, itis contemplated that the above-described registration steps can beperformed with the system placed in a (fixed) position and/ororientation corresponding to a position and/or orientation that thesystem would typically placed in during a tracking procedure. In caseswhere the associated system moves about the electromagnetic fieldgenerator (for example, a rotational C-arm), it is contemplated that theregistration process can be altered such that a plurality ofregistrations are performed with the associated system at a plurality ofpositions and/or orientations about the electromagnetic field generator.In such cases, it is further contemplated that the registrationcorresponding to any particular position and/or orientation of thesystem can be determined from either the registration from the positionand/or orientation among the plurality of positions and/or orientationsthat is closest to the current position and/or orientation, or aregistration that is interpolated from the plurality to provide anestimate of the registration at the current position and/or orientation.Alternatively, it is contemplated that the plurality of registrationscan be processed so as to “average” the location of corresponding pointsmeasured during the registration process. For example, it iscontemplated that each point can be measured in the world (tracker)coordinate system repeatedly at different positions and/or orientationsof the associated system. In this example, it is further contemplatedthat a representative position for each point (e.g., mean position) canbe used to compute the transform to the corresponding points in theimage coordinate system.

It is further contemplated that the method steps disclosed above can beemployed in various methods of treatment, as well as various methods ofimaging. For example, methods of the present invention comprise use ofelectromagnetic tracking systems disclosed herein with medical andsurgical procedures including, but not limited to, computer-assistedtherapy (CAT) and computer-assisted surgery (CAS), for example, tonavigate anatomical structures and target affected tissue, whileminimizing damage to healthy surrounding tissue; dental implantologyprocedures and treatments; functional endoscopic sinus surgery (FESS)for the removal of unwanted tissue in paranasal sinuses in order tofacilitate normal respiration, ventilation, and outflow for the patient;targeting tissue to be removed or treated, while navigating aroundanatomical structures in order to avoid injury to vulnerable structures;integration of robotics into medical and surgical procedures; preciselylocate and operate within and around the brain; orthopedic implants,orthopedic treatments and surgical procedures for repair and removal;acquisition of PET (positron emission tomography) information and usage;IGRT (image guided radiation therapy); soft tissue applications such asneedle biopsy, fine needle aspiration biopsy (FNAB); spinal surgery,ultrasound therapy and treatments, and transcranial magnetic stimulation(TMS) to trigger brain activity through the use of rapidly changingmagnetic fields, for example, in treating severe depression, mania, orauditory hallucinations (e.g. associated with schizophrenia).

In exemplary aspects, the electromagnetic field generator having acentral opening as described herein can comprise a Window FG (WFG,manufactured by NDI). However, it is contemplated that anyelectromagnetic field generator having a central opening and/or havingconsistently radio-translucent characteristics throughout its main body(e.g., central and lateral portions) as described herein can be usedwithin the disclosed electromagnetic tracking systems and methods.

It is contemplated that conventional EM field generators, such as, forexample and without limitation, the Aurora FG or table-top FG (NDI), canbe employed in the disclosed electromagnetic tracking systems andmethods. However, it should be appreciated that such conventional EMfield generators, which lack a central opening and radio-translucentcharacteristics, would confound many imaging procedures, includingposterior-anterior (PA) fluoroscopy, a fairly large range of obliqueviews, CT, CBCT, PET, and radiation therapy. Nonetheless, it iscontemplated that positioning of conventional EM field generators withina tracking system as described herein can achieve improvements in atleast accuracy and field of view.

It is contemplated that the disclosed apparatus and methods can includevarious components and features described in U.S. Pat. No. 7,103,931,U.S. Pat. No. 7,609,062, and U.S. Patent Publication No. 2011/0224537,the disclosures of which are hereby incorporated herein by reference intheir entirety.

EXPERIMENTAL EXAMPLES

The following examples are put forth so as to provide those of ordinaryskill in the art with a complete disclosure and description of how thecompounds, compositions, articles, devices and/or methods claimed hereinare made and evaluated, and are intended to be purely exemplary of theinvention and are not intended to limit the scope of what the inventorsregard as their invention. Efforts have been made to ensure accuracywith respect to numbers (e.g., amounts, temperature, etc.), but someerrors and deviations should be accounted for. Unless indicatedotherwise, parts are parts by weight, temperature is in C or is atambient temperature, and pressure is at or near atmospheric.

Example 1

The geometric accuracy (target registration error, TRE) of an exemplaryelectromagnetic tracking system including a field generator having acentral opening as described herein was compared to a conventional EMtracker without a central opening. Additionally, the x-ray compatibilityof the exemplary electromagnetic tracking system in combination with amobile C-arm for cone-beam CT (CBCT) was analyzed. Further, theimprovement in workflow associated with the incorporation of the fieldgenerator within a patient support table of the electromagnetic trackingsystem was examined.

TRE was measured for the Window FG and conventional Aurora FG using thetestbench in FIG. 3 for precise translation/rotation of a 6-DOF sensor(#610022) and registration phantom throughout the FOV. Although thebench and positioners were metallic, the trackers were mounted at aheight of about 100 cm to minimize EM field distortion. Angulardependence in TRE was observed for the 6-DOF sensor, so measurementswere performed with the sensor at about 45° to the cardinal axes. Inaddition, the sensor “indicator value” was recorded for each measurementto assess variability and EM field distortion. Measurements wereperformed with and without a carbon-fiber plate over the tracker tosimulate enclosure within a carbon-fiber OR table. As illustrated inFIG. 1( b), the registration phantom consisted of an acrylic rod andarray of divots translated across the bench. The phantom was CT scannedat high-resolution (0.6×0.6×0.3 mm³), with each divot localized in 3Dvisualization software (±0.1 mm) to establish ground truth. Registrationbetween the phantom and positioning system used fiducials distinct fromthe defined target divots. The 6-DOF tooltip was pivot-calibrated withtooltip offset error ±0.56 mm. Measurements were performed in coarseincrements (100 mm) throughout the full FOV and finer increments (25-50mm) along the central axes.

The Window FG was incorporated in a carbon-fiber OR table as shown inFIG. 3 to assess compatibility with fluoroscopy and CBCT. A prototypeC-arm for high-quality CBCT was used. Quantitative test phantoms forimage contrast, noise, and resolution were employed, along with ananthropomorphic head/body phantom. Fluoroscopic compatibility wasassessed as the range over which the EM field generator with the centralopening allowed an unattenuated beam to pass through the opening,including high-mag, isocentric, and low-mag C-arm positioning. CBCTcompatibility was assessed in images acquired with and without thecentral opening in the carbon-fiber table, characterized in terms oftruncation artifacts (noise and streaks) from out-of-field attenuationby the tracker.

An expert surgeon provided feedback regarding the integratedtracker-in-table concept in various application procedures, andpotential advantages were assessed in comparison to a conventionalover-table mount. The influence of metallic tools and C-arm wasassessed, and using the sensor indicator value to communicateinaccuracies within navigation software was investigated. Novel hybridtracker configurations included use of the Window FG with infraredand/or video-based trackers.

The fiducial registration error (FRE) between fiducials on the verticalphantom and divot targets was (1.12±0.39), (1.19±0.59), and (1.30±0.91)mm in (x,y,z) directions for the EM field generator having the centralopening, respectively, and (1.49±0.63), (0.96±0.44), (2.33±1.70) mm forthe conventional EM field generator (Aurora FG, NDI). As shown in FIG.8( a), the TRE measured from 10 repeat localizations was (1.43±0.77),(1.29±0.89), and (1.19±0.71) mm in (x,y,z) directions for the EM fieldgenerator having the central opening, respectively, and (1.28±0.51),(0.77±0.48), (1.49±0.86) mm for the conventional EM field generator. Aslight increase in TRE was observed for the EM field generator havingthe central opening near one FOV boundary (−y), and the EM fieldgenerator having the central opening exhibited superior TRE at greaterdepth (z). Overall, the magnitude and trend in TRE was similar for eachtracker, with the EM field generator having the central openingexhibiting slightly improved accuracy and FOV. There was no change inTRE measured with and without a carbon-fiber plate.

The central opening of the EM field generator was sufficiently large forunattenuated PA fluoroscopy at any level of magnification for the 30×30cm² detector. CBCT images acquired without and with the central openingunder the OR table are shown in FIG. 8( b). Although the FG enclosurewas visible in oblique projections, and only a simple (Gaussianextrapolation) truncation correction was applied, truncation artifactsarising from the EM field generator having the central opening wereminimal. A subtle increase in streak artifact is detectable, but theincrease in image noise was minimal (˜±2-5 HU) at the level of quantumnoise.

Expert surgeon feedback suggested a potentially important role for thetracker-in-table concept. The feedback noted clear logistical advantagesand x-ray compatibility compared to a conventional over-table mount.

Example 2 2.1 Electromagnetic Trackers

An exemplary EM field generator having a central opening was evaluatedin comparison to a conventional Aurora Field Generator (AFG, NDI) interms of tracking accuracy and FOV. As illustrated in FIG. 5, theexemplary EM field generator presents a large, central opening (about33×35 cm²) through which the x-ray beam may pass without attenuation(e.g., in a PA view), compared to the compact (andnon-radio-translucent) configuration of the AFG. The hollow sidebars ofthe exemplary EM field generator contained only three thin wires (in onesidebar only), with the sensor coil components enclosed in the barspositioned outside the x-ray beam. This setup gave a high level of x-raycompatibility for a large solid angle about the exemplary EM fieldgenerator, with electromagnetic components of the tracker lying outsidethe x-ray FOV and only the (nearly hollow) sidebars presenting in x-rayprojections from the semi-circular orbit of a rotational C-arm.

The current version of the AFG provides two preconfigured selections inFOV—a cube [500 mm side length, about 0.48 mm RMS geometric accuracy(for a 6 DOF (degrees of freedom) sensor)] and a cylindrical dome [960mm diameter, 660 mm depth, about 0.7 mm RMS geometric accuracy (6 DOFsensor)]. Stated RMS values have been supplied by the manufacturer. BothFOVs include an offset of the trackable area of 50 mm. The cube and domeFOV configurations have similar geometric accuracy in proximity to theFG, and the specified values refer to the average over the entire FOV.The nominal FOV provided by the EM field generator having the centralopening is a cylindrical dome (460 mm diameter, 650 mm depth including90 mm FOV offset from tracker) (see FIG. 7), and initialcharacterization of geometric accuracy was estimated to be 0.4 mm RMS (6DOF sensor). FIG. 6( b) gives an example of the dimensions of bothtracker embodiments.

FIG. 3 displays (a) the initial experimental configuration of theexemplary EM tracking system including the EM field generator having thecentral opening, (b) the prototype Tracker-in-Table incorporating the EMfield generator beneath a carbon-fiber OR tabletop, and (c) dimensionsof an exemplary under-table mount, the dotted line indicates the slidingdirection (unit: mm).

2.2 Geometric Accuracy of the WFG and AFG

A precise and reproducible linear positioning bench was built to allowmeasurement of TRE throughout the tracker FOV in an EM-compatibleenvironment. The measurement bench consisted of two linear translationstages, a 360-degree rotary table, and a custom TRE phantom (See FIG.6A). The two linear translation stages allowed adjustment of positionalong the y- and z-axis, and the TRE phantom itself provided adjustmentof position along the x-axis. The sensor exhibited a directionaldependence in measurements of TRE measured with the EM sensor. Allmeasurements reported below corresponded to a (1,1,0) angulation of thesensor (i.e., 45-degrees about the x and y axes) chosen asrepresentative of an “average” pose in routine use and minimizing biasin measurements in different directions (See FIG. 6C). The 360-degreerotary table was positioned in addition to the hand-driven linear tablesto adjust the orientation of the custom-built tool (45 degrees about thex axis). The linear table assembly had a specified precision of 0.1 mm,and the rotary table was specified to a precision of 0.1 degree. Anon-metallic (particle board) tracker support was built to elevate theentire FG approximately 80 cm above the surface of the bench to avoidfield distortion from the (metallic) benchtop. The TRE phantom was builtfrom non-metallic materials (acrylic and polyethylene) to avoiddistortion of the EM field. The phantom included sixteen divots alongthe x-axis for TRE measurement and sixteen pairs of bars forreproducible positioning of the EM sensor plug (See FIG. 6C). The EMsensor was a 6 DOF Standard Reference Marker provided by themanufacturer consisting of two embedded 5 DOF sensors, showing improvedtracking accuracy compared to a single 5 DOF sensor. The sixteen divotswere attached at 5 cm spacing in a co-linear manner along the x-axis.Four mounting holes on the inferior plate of the TRE phantom wereprecisely manufactured to fit with the four mounting holes on the rotarytable. A computed tomography (CT) scan of the TRE phantom was acquired(0.64×0.64×1.00 mm³), and divots were localized to sub-voxel accuracy(˜0.1 mm) for the four mounting holes by repeat localization (six timesaveraged) and tri-planar slice interpolation in the image guidancesystem. Point-based registration was performed to register the CT scanof the TRE phantom (reference frame—F_(CT)) to the lower mounting holeson the bench assembly using the physical position of the four mountingholes of the TRE phantom matching those on the rotary table (F_(Stage)).Following point-based registration, the relationship between the trackermeasurements in the CT reference frame and the stage coordinates(alternatively referred to as the world coordinate system) could bedetermined as:

F _(Stage) =T _(Stage) ^(CT) ·F _(CT),

where T_(Stage) ^(CT) defines the transformation matrix between positionvectors in the two reference frames.

To determine the correct position of the tracker measurements in theworld coordinate system, it was necessary to add or subtract an offsetcorresponding to the benchtop assembly to the coordinates of each divotobtained in F_(CT) and transformed to F_(Stage). Writing the i^(th)divot measurement on the TRE phantom as {right arrow over (d)}_(CT)^(i)=(x_(i), y_(i), z), its physical position, {right arrow over(t)}_(Stage) ^(i) was obtained as:

{right arrow over (t)} _(Stage) ^(i) =T _(Stage) ^(CT) ·{right arrowover (d)} _(CT) ^(i)+{right arrow over (α)}_(Stage)

where {right arrow over (α)}_(Stage) is a three-dimensional

${\overset{\rightarrow}{\alpha}}_{Stage} = {\begin{bmatrix}0 \\{\Delta \; y} \\{\Delta \; z}\end{bmatrix}.}$

and Δy and Δz denote adjustments of the linear slider in y and zdirections.

Therefore, for each measurement location two corresponding points weredetermined: a physical measurement of the sensor tip position and theposition of the sensor tip in the image guidance software. Through theestablished transformation matrix, the points can be moved into a commonreference frame and TRE expressed as the Euclidian distance between thepoints.

FIG. 6( a) provides a schematic of the benchtop setup for measurement oftracker accuracy. The exemplary EM field generator having the centralopening and the AFG were placed on a non-metallic (wooden) support,which was mounted to a precise 3D positioning table. Linear stagesallowed localization of the 6 DOF EM sensor plug throughout and beyondthe tracker FOV. The linear table assembly enabled y- and z-axis motion,and the TRE phantom provided positioning of a pointer in divots alongthe x-axis in the tracker coordinate system. FIG. 6( b) illustrates theshape and dimensions of the Aurora FG (front left) and the EM fieldgenerator having the central opening (back right, unit: mm). FIG. 6( c)illustrates the 6 DOF EM sensor mounted on the TRE phantom using rigidposts and a “divot” hole at discrete locations along the x-axis. Thesensor was attached to a connector plate at a 45° angle, giving anintermediate pose approximating freehand use (not aligned with anyparticular axis). The connector plate included a conical pointer thatfit tightly into the “divot” holes, and two through holes that fit theTRE phantom on rigid posts on the x-axis upright. This setup providedreproducible placement of the 6 DOF sensor.

2.3 Implementation of the WFG in a Preclinical C-Arm OR Setup

2.3.1 Prototype OR Table

A Tracker-in-Table configuration was implemented as illustrated in FIG.3. A custom carbon fiber OR tabletop (CFI Medical Solutions, Fenton,Mich. USA) was mounted to a 3-DOF metallic OR table base. The influenceof the carbon fiber table on tracking accuracy was found to benegligible (<0.1 mm) by repeating TRE measurements with and without thetabletop on the bench. The custom OR table included acrylic railsattached underneath to support the EM field generator having the centralopening. The rails (each 70 mm×850 mm at 480 mm separation) were builtfrom acrylic plates and plastic screws to avoid EM field distortion. Therails allowed width adjustment and (manual) longitudinal positioning ofthe exemplary EM field generator under the table with set-screws to fixthe field generator in a desired position.

2.3.2 Tracking Accuracy in the Presence of a Mobile C-Arm

The tracking accuracy of the EM field generator having the centralopening in the Tracker-in-Table prototype was evaluated in the contextof C-arm CBCT-guided surgery. The setup included an anthropomorphicchest (The Phantom Laboratory, Greenwich, N.Y. USA) placed in proneposition (FIG. 1 a). Conical divots drilled on the phantom surface wereused separately as registration fiducials (for image-world registration)and target points (for measurement of TRE). The tip of the EM pointertool (Aurora 6 DOF straight tip pointer tool, 65 mm long, 3 mm diameter)gave a tight fit to the divots, allowing reproducible positioning of thetool tip, and the conical divots were easily discerned in CT images. Adistinct set of surface divots was used as target points in measuringTRE. The divots allowed reproducible positioning of the pointer tool tipand could be easily discerned in CT images. In total, 36 divots on thephantom were selected for measurements—9 selected for purposes ofimage-world registration and 27 selected as target points for analysisof TRE. The 9 registration points were selected as the set (over allpossible combinations) that minimized target registration error. Thephantom allowed implantation and removal of thoracic and lumbar pediclescrews. The prototype mobile C-arm for CBCT was developed incollaboration with Siemens Healthcare as described in previous work. Itis based on an isocentric mobile C-arm (Powermobil, Siemens, Erlangen,Germany) modified to include a large-area flat-panel detector (PaxScan3030+, Varian Imaging Products, Palo Alto Calif.), a motorized orbitaldrive, a method for geometric calibration, and a computer control systemfor image acquisition and 3D reconstruction. The C-arm provides avolumetric FOV (˜15×15×15 cm³) with sub-mm 3D spatial resolution,soft-tissue visibility, and generation of CBCT images (512³ or 256³)within ˜15 seconds after completion of a scan. The prototype mobileC-arm has been evaluated in the context of orthopaedic (spine) surgery,focusing on image quality and radiation dose in image-guided procedures;cochlear implant; sinus and skull-base surgery, focusing on improvedsurgical precision in tumor surgery adjacent to critical structures;thoracic surgery, brachytherapy; and guidance of tibial plateau fracturereduction. Stationary C-arms are entering broad use in cardiovascularinterventions.

The geometric accuracy of the EM field generator having the centralopening was assessed in five distinct scenarios: 1.) without the C-armand without spine screws; 2.) without the C-arm but with three spinescrews in the phantom; 3.) with the C-arm in Lateral (LAT) orientationand with three spine screws in the phantom; 4.) with the C-arm inPosterior-Anterior (PA) orientation and without spine screws in thephantom; and 5.) with the C-arm in PA orientation and with three spinescrews in the phantom.

2.3.3 Effect of the EM Field Generator Haying the Central Opening onCBCT Image Quality

CBCT image quality can be degraded by objects located outside thevolumetric FOV, typically in the form of streaks artifacts. The EM fieldgenerator having the central opening is located outside the CBCT FOV andit presents fairly low attenuation, and was therefore anticipated tohave fairly small effect on 3D image quality. The influence of the EMfield generator having the central opening on CBCT image quality wasassessed in quantitative and qualitative phantoms. All scans were at thenominal technique previously identified for thoracic scanning: 100 kVp,230 mAs, and 200 projection images, corresponding to 4.61 mGy dose atthe center of a 32 cm body phantom.

Quantitative evaluation involved a QRM Thorax Phantom (Quality Assurancein Radiology and Medicine GmbH, Erlangen, Germany). The phantom wascustomized to allow placement of an acrylic cylinder containing fourtissue-equivalent inserts in the middle of the phantom. The 10 cmacrylic cylinder holder has an electron density relative to water ofρ_(e)=1.15 and approximately 130 HU, and the tissue-equivalent insertsincluded: solid water (ρ_(e)=0.99, 0 HU), breast (ρ_(e)=0.96, −41 HU),liver (ρ_(e)=1.07, 83 HU), and adipose (ρ_(e)=0.93, −84 HU), each havinga diameter of 28 mm (Gammex RMI, Madison Wis.). Soft tissue CNR wasmeasured to compare CBCT image quality with and without theTracker-in-Table. The contrast (signal difference) was given by thedifference in attenuation coefficient between a structure of interestand the background, and the noise was given by the standard deviation invoxel values. The CNR is therefore:

${{CNR} = \frac{{\mu_{I} - \mu_{B}}}{\left( {\sigma_{I} + \sigma_{B}} \right)/2}},$

where μ_(I) and μ_(B) denote the average voxel value in material “I”(i.e., the structure of interest for example, a given soft-tissue insertin the QRM phantom) and the background “B” (e.g., the acrylic holder inthe QRM phantom). Similarly, σ_(I) and σ_(B) denote the standarddeviation in voxel values within the insert and background,respectively.

Qualitative evaluation involved the anthropomorphic chest phantom withspine screws in place (viz., a translaminar screw (T1) and two pediclescrews (T5 and T7)). The spine screws were composed of metal (titaniumand steel), which in themselves are expected to produce CBCT imageartifacts separate from the out-of-field truncation artifacts possiblyintroduced by the Tracker-in-Table. The effects on image quality (i.e.,CBCT images of the phantom with spine screws, imaged with and withoutthe EM field generator having the central opening in the table) andworkflow were assessed qualitatively by an experienced andfellowship-trained spine surgeon.

3. Results

3.1 Geometric Accuracy

For both (a) the EM field generator having the central opening and (b)the AFG tracking systems, the FOV was evaluated first by measuring TREin coarse increments of 10 cm in (x, y, z). A total of (5×5×5) suchmeasurements were made across about (50×50×50) cm³ and repeated tentimes, averaged, and transformed into reference frame F_(Stage) forevaluation of TRE. The measurements (n=250) were performed using apointer tool calibrated prior to data acquisition. The distance betweenthe measured and actual pointer position included possible (likelysmall) pointer calibration errors in the resulting TRE, so the reportedvalues may represent a small overestimate of the actual TRE associatedwith just the tracker (independent of the pointer calibration error). Asshown in FIG. 9, the TRE varied across the FOV, most notably in the z(depth) direction. For the EM field generator having the centralopening, the TRE (as a function of z) was: 0.91±0.52 mm (at z=134±4.1mm); 1.00±0.51 mm (at z=235.1±4.1 mm); 1.50±0.64 mm (at z=335.3±4.3 mm);2.45±0.93 mm (at z=436.0±4.5 mm); and 3.66±1.56 mm (at z=537.5±5.1 mm).Overall, the measurements show a trend of gradually increasing TRE atgreater depth, with a mean TRE across the evaluated FOV of 1.90±1.38 mm.Although the farthest measurement was inside the specified FOV, the TREwas seen to increase steeply at the FOV boundaries. Similar evaluationsperformed for the AFG showed a mean TRE of 2.17±1.91 mm. Statisticalanalysis on the results, using Student's t-test, showed no significantdifference between the EM field generator having the central opening andthe AFG (p=0.32).

Measurement of TRE at finer increments in x, y, and z was performed at2.5 cm increments on the central y-axis and z-axis, and at 5 cm spacingon the central x-axis for both the EM field generator having the centralopening and the AFG, each measured ten times. Results are summarized inFIG. 10. The mean TRE along the x-axis for the EM field generator havingthe central opening was 1.43±0.77 mm, compared to 1.28±0.51 mm for theAFG. The mean TRE along the y-axis of the EM field generator having thecentral opening was 1.29±0.89 mm, compared to 0.77±0.48 mm for the AFG.The measurements showed an anomalous, gradual increase in TRE for the EMfield generator having the central opening near one FOV boundary (−y),increasing from ˜0.5 mm to ˜3.9 mm within ˜150 mm of the FOV edge. Thegradual increase was contrary to the sharper increase in TRE at the FOVedge seen for the +x direction [FIG. 10( a)]. Discussions with themanufacturer suggested a small error in the internal calibration of theprototype as a possible explanation, and one that could be rectified byfactory recalibration. The mean TRE along the z-axis was 1.19±0.79 mmfor the EM field generator having the central opening and 1.13±0.72 mmfor the AFG. As summarized in FIG. 5, the overall TRE was slightlyimproved for the AFG, although the EM field generator having the centralopening demonstrated superior accuracy at greater z-axis depth. Overallmean TRE was 1.28±0.79 for the EM field generator having the centralopening, and 1.13±0.72 for the AFG. Thus, with reference to FIG. 10, thetrackers exhibited similar geometric accuracy, although the EM fieldgenerator having the central opening exhibited a somewhat deeper FOV(z-direction) than the AFG.

3.2 Implementation of Tracker-in-Table in a Preclinical Setup

3.2.1 Tracking Accuracy

Tracker registration was performed in each of six scenarios: (1) withouteither the C-arm or spine screws; (2) without the C-arm but with thethree spine screws implanted; (3) with the C-arm in LAT orientation(with spine screws in place); (4) with the C-arm in PA orientation (nospine screws); (5) with the C-arm in PA orientation (with spine screwsin place); and (6) a combination of setup (3) and (4)—effectivelyachieving an average of registrations in LAT and PA C-arm orientations.The average registration was calculated as follows: the fiducial pointmeasurements were performed separately in configurations (3) and (4),and the two measured locations (in the tracker coordinate system,F_(Tracker)) of the same fiducial were averaged; subsequently, thepoint-based tracker-to-image registration in the CT coordinate system,F_(CT), was computed using the averaged coordinates of the fiducials(FIG. 11). Results showed negligible (<0.1 mm difference) effect of thespine screws on registration accuracy (presumably due to negligibledistortion of the EM field); therefore, results for the registrationscenarios “with spine screws” and “with the C-arm in LAT orientation (nospine screws)” are not shown (equivalent to (1) and (4), respectively).

As depicted in FIG. 11, good geometric accuracy was achieved under thesimple case in which tracker registration was performed in the absenceof the C-arm (corresponding to measurement scenario (1)), where TRE was0.39±0.43 mm. Introduction of spine screws (scenario 2) increased TREslightly to 0.60±0.21 mm. Under the same registration scenario (1),introducing the C-arm in LAT orientation (scenario 3) increased the TREsignificantly to 0.83±0.43 mm. More severe degradation in accuracy wasobserved with the C-arm in PA orientation, giving TRE of 2.10±0.38 mmand 2.26±0.38 mm in scenarios (4) and (5), respectively. These resultsshow that although the performance of the EM field generator having thecentral opening was not degraded by a handful of spine screws in theFOV, the presence of the C-arm caused significant distortion—especiallyin PA orientation—and motivated alternative registration scenarios.

FIG. 11 also shows results for such a modified registration scenario,where tracker-image registration was computed with the C-arm in LATorientation (3). The accuracy is accordingly improved in thecorresponding measurement scenario (3), with TRE of 0.58±0.27 mm. TheTRE in scenarios (1) and (2) was essentially the same as in the previouscase. However, placement of the C-arm in the PA orientation again metwith significantly degraded TRE of 2.14±0.32 mm and 2.24±0.35 mm forscenarios (4) and (5), respectively.

FIG. 11 shows analogous results for registration scenario (4) in whichtracker-image registration was computed with the C-arm in PAorientation. The accuracy was accordingly improved in the correspondingmeasurement scenario (4) and (5)—TRE of 0.92±0.41 mm and 1.04±0.39 mm,respectively—but accuracy was degraded when the C-arm moved to LATorientation (3) or when removed from tableside (1) or (2). The resultsof scenario (3), together with those of scenario (2), suggest thataccurate tracking could be achieved only under conditions correspondingclosely to those at the time of registration. While the TRE resulting inalternative conditions is arguably acceptable (about 2-3 mm) for someguidance applications, the results motivated further investigation of aregistration scenario that could offer robust tracking at any C-armorientation.

A reasonable compromise in registration accuracy was found inregistration scenario (5), with results shown in FIG. 11. Thisregistration scheme uses a set of corresponding registration fiducialpoints measured with the C-arm in both PA and LAT position. The averageposition for each fiducial point was determined and subsequently used inthe point-based registration method. The results show reasonablyaccurate (<2 mm) TRE across all scenarios (although none are as accurateas the ideal case). Using the “average” registration, TRE in the range1.0-1.5 mm was achieved with or without the C-arm and with the C-arm atany angulation.

An alternative scenario involves a plurality of tracker-to-imageregistrations and selection of the registration most closelycorresponding to the current position and/or orientation of the trackerand associated C-arm (or other system). A further alternative involvesuse of a registration interpolated from a plurality of suchregistrations as an estimate of a tracker-to-image transformation.

FIG. 11 provides box-and-whisker plots representing: the median TRE(horizontal line), the 25th and 75th percentiles (edges of the box), andtotal range (extent of whiskers) excluding outliers (•symbols), withoutliers defined as greater than 1.5*inter-quartile range below thefirst or above the third quartile. The column at right illustrates fourof the five registration scenarios detailed in the text involvingvarious C-arm orientations with and without spine screws. Registrationscenario #2 was omitted, since it was found equivalent to scenario #1.The presence of the C-arm had a significant impact on tracker accuracy,and no single, simple registration scenario was found that provided lowTRE for all setups. However the “average” registration scenario wasfound to give fairly good TRE (˜1.0-1.5 mm) irrespective of the C-armorientation, suggesting a practical method for maintaining trackeraccuracy in the presence of the C-arm.

3.2.2 Effect of the WFG on CBCT Image Quality

For fluoroscopic imaging, the central opening of the exemplaryelectromagnetic field generator allows the x-ray beam to pass withoutattenuation in the PA view. In oblique or LAT views, the hollow sidebars of the exemplary electromagnetic field generator are visible aslongitudinal shadows in the projection but are at the same level ofcontrast as the edges of the OR table and were not considered adetriment to fluoroscopic image quality.

Each phantom (QRM Thorax phantom and the anthropomorphic chest phantom,including three spine screws in the T1, T5, and T7 vertebrae) wasscanned on the CBCT C-arm with and without the exemplary electromagneticfield generator under the OR table. As shown in FIG. 12, the presence ofthe exemplary electromagnetic field generator having the central openingintroduced appreciable streak artifacts comparable in magnitude torelevant soft-tissue contrasts. The artifacts impart an increase innoise in the form of streak artifacts directed approximately toward the5 o'clock and 7 o'clock directions in FIG. 12( b), consistent with thelocation of the side-bars of the exemplary electromagnetic fieldgenerator outside the 3D field of view.

The effect on image quality was analyzed quantitatively in terms of CNRin the various tissue-equivalent inserts in the QRM phantom shown inFIG. 12. CBCT images were acquired under three configurations toidentify the source of the streak artifacts: i.) the OR table alone;ii.) the table with acrylic support rails underneath (but without thetracker); and iii.) the table, support rails, and the exemplaryelectromagnetic field generator having the central opening. The acrylicsupport rails under the OR table were found to impart a small butmeasurable level of streak artifact, reducing the CNR in soft-tissueinserts by ˜10%. The major source of artifacts was, however, theside-bars of the exemplary electromagnetic field generator itself.Although the side-bars are nominally hollow (with just three thin wiresrunning in one arm connecting the EM coils), the material of theside-bars is fairly dense, and the shape of the side-bars is sub-optimal(rectangular, rather than rounded). As a result, the streak artifactsshown in FIG. 7 had an appreciable effect on soft-tissue detectability,reducing CNR by ˜15% to 37% depending on the location in the FOV. Sharpedges in the projection data (e.g., the sharp corners of the sidebars)are associated with increased streaks in CBCT reconstructions due toview sampling effects and accentuation by the ramp filter in filteredbackprojection. Thus, it is contemplated that re-engineering of the sidebars of exemplary electromagnetic field generator using a lighter androunded shape can improve image quality in soft-tissue imaging tasks.

The anthropomorphic chest phantom with spine screws (T1, T5, and T7)inserted was scanned without and with the Tracker-in-Table. Evaluationfocused on the effect of streak artifacts in the context ofhigh-contrast anatomy (bones) under conditions of artifacts typical ofinterventional imaging (i.e., streak and beam hardening in the presenceof pedicle screws). As shown in FIG. 13, although the same streakartifacts arising from the Tracker-in-Table were detectable in theimages, the spine screws were clearly distinguishable, and the overalldegradation in the ability to perform high-contrast visualization taskswas minimal. Image subtraction was performed between images in FIGS. 13(a) and 13(d) to evaluate the relative magnitude of streak artifacts,which generally manifest as higher intensities than the surroundingstructures. Results showed the streak artifact intensities to be in therange of (or slightly higher than) the contrast of simulated softtissue. This places the magnitude of the streak artifacts in the rangeof soft-tissues, potentially degrading soft-tissue visibility as shownin FIG. 12, but with fairly small effect on high-contrast structurevisibility in FIG. 13.

CBCT images (FIGS. 13 a-c) without and (FIGS. 13 d-f) with theTracker-in-Table were recorded. In (b, c, e, and f) the metallic pediclescrew (purposely placed in the anthropomorphic phantom with a slightmedial breach of the spinal canal) created a significant degree ofstreak artifact, but the streaks associated with the exemplaryelectromagnetic field generator having the central opening were fairlysmall relative to high-contrast (bone) anatomical visualization and didnot further impede the task of assessing screw placement (i.e.,detection of canal breach).

Although several embodiments of the invention have been disclosed in theforegoing specification, it is understood by those skilled in the artthat many modifications and other embodiments of the invention will cometo mind to which the invention pertains, having the benefit of theteaching presented in the foregoing description and associated drawings.It is thus understood that the invention is not limited to the specificembodiments disclosed hereinabove, and that many modifications and otherembodiments are intended to be included within the scope of the appendedclaims. Moreover, although specific terms are employed herein, as wellas in the claims which follow, they are used only in a generic anddescriptive sense, and not for the purposes of limiting the describedinvention, nor the claims which follow.

What is claimed is:
 1. An electromagnetic tracking system comprising: apatient support table having a longitudinal axis, a transverse axis, anda patient contact surface, the transverse axis of the patient supporttable being substantially perpendicular to the longitudinal axis of thepatient support table; and an electromagnetic field generatoroperatively coupled to the patient support table, the electromagneticfield generator being selectively moveable along at least one of thelongitudinal axis and the transverse axis of the patient support table,wherein the electromagnetic field generator has a lower surface and anupper surface, and wherein the electromagnetic field generator defines acentral opening through the lower surface and the upper surface, whereinthe patient contact surface of the patient support table is superposedrelative to at least a portion of the electromagnetic field generator.2. The electromagnetic tracking system of claim 1, wherein theelectromagnetic field generator is integrally positioned within thepatient support table.
 3. The electromagnetic tracking system of claim1, wherein the patient support table comprises a pair of spaced bracketsextending substantially parallel to the longitudinal axis of the patientsupport table, and wherein the pair of spaced brackets are configured toslidingly receive the electromagnetic field generator.
 4. Theelectromagnetic tracking system of claim 1, wherein the patient supporttable comprises a pair of spaced brackets extending substantiallyparallel to the transverse axis of the patient support table, andwherein the pair of spaced brackets are configured to slidingly receivethe electromagnetic field generator.
 5. The electromagnetic trackingsystem of claim 1, wherein the electromagnetic field generator comprisesa first coil assembly and a second coil assembly, the first coilassembly being in electrical communication with the second coilassembly, wherein the first coil assembly is oriented substantiallyparallel to the second coil assembly, and wherein the first coilassembly is spaced in opposition to the second coil assembly across thecentral opening of the electromagnetic field generator.
 6. Theelectromagnetic tracking system of claim 5, wherein the first and secondcoil assemblies of the electromagnetic field generator respectivelycomprise a plurality of coils that are spaced apart in a directionsubstantially parallel to the longitudinal axis of the patient supporttable.
 7. The electromagnetic tracking system of claim 5, wherein thefirst and second coil assemblies of the electromagnetic field generatorrespectively comprise a plurality of coils that are spaced apart in adirection substantially parallel to the transverse axis of the patientsupport table.
 8. The electromagnetic tracking system of claim 5,wherein the electromagnetic field generator comprises first and secondcoil housing arms and first and second side arms that cooperate todefine the central opening of the electromagnetic field generator,wherein the first coil assembly is positioned within the first coilhousing arm and the second coil assembly is positioned within the secondcoil housing arm, and wherein the first and second side arms areconnected to and oriented substantially perpendicular to the first andsecond coil housing arms.
 9. The electromagnetic tracking system ofclaim 8, wherein the first and second side arms of the electromagneticfield generator are substantially hollow.
 10. The electromagnetictracking system of claim 9, further comprising a radiation source, theradiation source being configured to selectively transmit radiation,wherein the radiation source is positioned such that radiation istransmittable through at least one of (a) the central opening of theelectromagnetic field generator and (b) the first and second side armsof the electromagnetic field generator.
 11. The electromagnetic trackingsystem of claim 8, wherein the first and second side arms each haverespective side edges, and wherein at least a portion of the side edgesof the first and second side arms are rounded.
 12. The electromagnetictracking system of claim 2, wherein the electromagnetic field generatorcomprises a plurality of coils, and wherein the plurality of coils arespaced about a periphery of the patient support table.
 13. Theelectromagnetic tracking system of claim 12, wherein the patient supporttable is selected from the group consisting of a surgical operatingtable, an interventional radiology table, a computed tomography (CT)scanner, a positron emission tomography (PET) scanner, and aradiotherapy patient table.
 14. An electromagnetic tracking systemcomprising: a patient support element having a longitudinal axis, atransverse axis, and a patient contact surface, the transverse axis ofthe patient support element being substantially perpendicular to thelongitudinal axis of the patient support element; and an electromagneticfield generator, the electromagnetic field generator being selectivelymoveable along at least one of the longitudinal axis and the transverseaxis of the patient support element, wherein the patient contact surfaceof the patient support element is superposed relative to at least aportion of the electromagnetic field generator.
 15. The electromagnetictracking system of claim 14, wherein the electromagnetic field generatoris operatively coupled to the patient support element.
 16. Theelectromagnetic tracking system of claim 14, wherein the electromagneticfield generator is integrally positioned within the patient supportelement.
 17. The electromagnetic tracking system of claim 15, whereinthe patient support element comprises a patient support table.
 18. Theelectromagnetic tracking system of claim 17, wherein the patient supporttable comprises a pair of spaced brackets extending substantiallyparallel to the longitudinal axis of the patient support table, andwherein the pair of spaced brackets are configured to slidingly receivethe electromagnetic field generator.
 19. The electromagnetic trackingsystem of claim 17, wherein the patient support table comprises a pairof spaced brackets extending substantially parallel to the transverseaxis of the patient support table, and wherein the pair of spacedbrackets are configured to slidingly receive the electromagnetic fieldgenerator.
 20. The electromagnetic tracking system of claim 18, whereinthe electromagnetic field generator has an lower surface and an uppersurface, and wherein the electromagnetic field generator defines acentral opening through the lower surface and the upper surface.
 21. Theelectromagnetic tracking system of claim 20, wherein the electromagneticfield generator comprises a plurality of coils spaced about the centralopening of the electromagnetic field generator, wherein the spacing ofthe plurality of coils about the central opening is configured to permittransmission of radiation through the central opening without contactingthe plurality of coils.
 22. The electromagnetic tracking system of claim20, wherein the electromagnetic field generator comprises a first coilassembly and a second coil assembly, the first coil assembly being inelectrical communication with the second coil assembly, wherein thefirst coil assembly is oriented substantially parallel to the secondcoil assembly, and wherein the first coil assembly is spaced inopposition to the second coil assembly across the central opening of theelectromagnetic field generator.
 23. The electromagnetic tracking systemof claim 22, wherein the first and second coil assemblies of theelectromagnetic field generator respectively comprise a plurality ofcoils that are spaced apart in a direction substantially parallel to thelongitudinal axis of the patient support table.
 24. The electromagnetictracking system of claim 22, wherein the first and second coilassemblies of the electromagnetic field generator respectively comprisea plurality of coils that are spaced apart in a direction substantiallyparallel to the transverse axis of the patient support table.
 25. Theelectromagnetic tracking system of claim 22, wherein the electromagneticfield generator comprises first and second coil housing arms and firstand second side arms that cooperate to define the central opening of theelectromagnetic field generator, wherein the first coil assembly ispositioned within the first coil housing arm and the second coilassembly is positioned within the second coil housing arm, and whereinthe first and second side arms are connected to and orientedsubstantially perpendicular to the first and second coil housing arms.26. The electromagnetic tracking system of claim 25, wherein the firstand second side arms of the electromagnetic field generator aresubstantially hollow.
 27. The electromagnetic tracking system of claim26, wherein the first and second side arms each have respective sideedges, and wherein at least a portion of the side edges of the first andsecond side arms are rounded.
 28. The electromagnetic tracking system ofclaim 18, wherein the electromagnetic field generator comprises one ormore radio-translucent materials.
 29. The electromagnetic trackingsystem of claim 28, wherein the electromagnetic field generatorcomprises a radio-translucent sheet having a periphery surrounding acentral region, and wherein the electromagnetic field generator furthercomprises plurality of coils spaced about the central region within theperiphery of the radio-translucent sheet, wherein the spacing of theplurality of coils about the central region is configured to permittransmission of radiation through the central region without contactingthe plurality of coils.
 30. The electromagnetic tracking system of claim14, further comprising a radiation source.
 31. The electromagnetictracking system of claim 30, wherein the electromagnetic field generatoris integrally connected to the radiation source.
 32. An electromagnetictracking method, comprising: positioning a patient on a patient supporttable, the patient support table having a longitudinal axis, atransverse axis, and a patient contact surface, the transverse axis ofthe patient support table being substantially perpendicular to thelongitudinal axis of the patient support table; positioning anelectromagnetic field generator such that the patient contact surface ofthe patient support table is superposed relative to at least a portionof the electromagnetic field generator, the electromagnetic fieldgenerator operatively coupled to the patient support table; selectivelymoving the electromagnetic field generator along at least one of thelongitudinal axis and the transverse axis of the patient support table;positioning a radiation source at a selected orientation relative to theelectromagnetic field generator, the radiation source being configuredto selectively transmit radiation toward the patient; selectivelyactivating the radiation source; and selectively activating theelectromagnetic field generator.
 33. The electromagnetic tracking methodof claim 32, wherein the electromagnetic field generator has a lowersurface and an upper surface, wherein the electromagnetic fieldgenerator defines a central opening through the lower surface and theupper surface, and wherein the step of positioning the radiation sourceat a selected orientation relative to the electromagnetic fieldgenerator comprises positioning the imaging device such that radiationfrom the imaging device is selectively transmittable through the centralopening of the electromagnetic field generator.
 34. The electromagnetictracking method of claim 32, wherein the electromagnetic field generatorhas a lower surface and an upper surface, wherein the electromagneticfield generator comprises first and second coil housing arms and firstand second side arms that cooperate to define a central openingextending through the lower surface and the upper surface of theelectromagnetic field generator, a first coil being positioned withinthe first coil housing arm and a second coil being positioned within thesecond coil housing arm, the first coil being in electricalcommunication with and oriented substantially parallel to the secondcoil, wherein the first and second side arms are connected to andoriented substantially perpendicular to the first and second coilhousing arms, wherein the first and second side arms of theelectromagnetic field generator are substantially hollow, and whereinthe step of positioning the imaging device at a selected orientationrelative to the electromagnetic field generator comprises positioningthe imaging device such that radiation from the radiation source isselectively transmittable through at least one of (a) the centralopening of the electromagnetic field generator and (b) the first andsecond side arms of the electromagnetic field generator.
 35. Theelectromagnetic tracking method of claim 32, further comprisingselectively moving the electromagnetic field generator along at leastone of the longitudinal axis and the transverse axis of the patientsupport table.
 36. The electromagnetic tracking method of claim 32,wherein the step of moving the electromagnetic field generator comprisesmanually moving the electromagnetic field generator.
 37. Theelectromagnetic tracking method of claim 32, wherein the step of movingthe electromagnetic field generator comprises, by a computer, moving theelectromagnetic field generator in an automated fashion depending uponthe monitored position of a surgical tool.
 38. The electromagnetictracking method of claim 32, wherein the radiation source comprises aC-arm, the method further comprising: positioning the C-arm at a firstposition and orientation relative to the patient; positioning a surgicaltool at a first position relative to the patient; using a firstcoordinate system associated with the patient support table, determininga first coordinate set indicative of the first position of the surgicaltool; using a second coordinate system associated with the C-arm,determining a second coordinate set indicative of the first position ofthe surgical tool; and calculating a transformation suitable fordetermining a coordinate set from the first coordinate system thatcorresponds to a coordinate set from the second coordinate system.
 39. Amethod of treatment comprising: positioning a patient on a patientsupport table, the patient support table having a longitudinal axis, atransverse axis, and a patient contact surface, the transverse axis ofthe patient support table being substantially perpendicular to thelongitudinal axis of the patient support table; positioning anelectromagnetic field generator such that the patient contact surface ofthe patient support table is superposed relative to at least a portionof the electromagnetic field generator, the electromagnetic fieldgenerator operatively coupled to the patient support table; selectivelymoving the electromagnetic field generator along at least one of thelongitudinal axis and the transverse axis of the patient support table;positioning a radiation source at a selected orientation relative to theelectromagnetic field generator, the radiation source being configuredto selectively transmit radiation toward the patient; selectivelyactivating the radiation source; and selectively activating theelectromagnetic field generator.
 40. A method of imaging comprising:positioning a patient on a patient support table, the patient supporttable having a longitudinal axis, a transverse axis, and a patientcontact surface, the transverse axis of the patient support table beingsubstantially perpendicular to the longitudinal axis of the patientsupport table; positioning an electromagnetic field generator such thatthe patient contact surface of the patient support table is superposedrelative to at least a portion of the electromagnetic field generator,the electromagnetic field generator operatively coupled to the patientsupport table; selectively moving the electromagnetic field generatoralong at least one of the longitudinal axis and the transverse axis ofthe patient support table; positioning a radiation source at a selectedorientation relative to the electromagnetic field generator, theradiation source being configured to selectively transmit radiationtoward the patient; selectively activating the radiation source;selectively activating the electromagnetic field generator; andselectively recording an image of the patient.